PRINCIPAL CONSULTANT - LIFESCIENCES

Key Responsibilities: 14 years of experience in Life Sciences with CSV Validation for GxP systems Serve as a subject matter expert for Quality Engineering practice on IT systems and solutions including Clinical Trial Management Systems CTMS Veeva CTMS Medidata Rave Oracle Siebel Regulatory Platforms Veeva Vault RIM Veeva Vault Laboratory Information Management Systems LIMS LabVantage LabWare STAR LIMS Supply Chain Kinaxis Knowledge of key Pharma regulations including 21 CFR Part 11 EU Annex 11 … This is a short preview. Tap Apply to read the full job description and apply on the employer's or recruiter's page.